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Alignment of Nanoplates in Lamellar Diblock Copolymer Domains and the Effect of Particle Volume Fraction on Phase Behavior

机译:纳米层板在层状二嵌段共聚物结构域中的对准及颗粒体积分数对相行为的影响

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Polymer nanocomposites (PNCs) that employ diblock copolymers (BCPs) to organize and align anisotropic nanoparticles (NPs) have the potential to facilitate self-assembling hierarchical structures. However, limited studies have been completed to understand the parameters that guide the assembly of nonspherical NPs in BCPs. In this work, we establish a well-defined nanoplate system to investigate the alignment of two-dimensional materials in a lamellar-forming poly(styrene-b-methyl methacrylate) (PS-b-PMMA) BCP with domains oriented parallel to the substrate. Monodisperse gadolinium trifluoride rhombic nanoplates doped with ytterbium and erbium [GdF3:Yb/Er (20/2 mol %)] are synthesized and grafted with phosphoric acid functionalized polyethylene glycol (PEG-PO(3)H2). Designed with chemical specificity to one block, the nanoplates align in the PMMA domain at low volume fractions (phi = 0.0083 and phi = 0.017). At these low NP loadings, the BCP lamellae are ordered and induce preferential alignment of the GdF3:Yb/Er nanoplates. However, at high volume fractions (phi = 0.050 and phi = 0.064), the BCP lamellae are disordered with isotropically dispersed nanoplates. The transition from an ordered BCP system with aligned nanoplates to a disordered BCP with unaligned nanoplates coincides with the calculated overlap volume fraction, phi* = 0.051, where the pervaded space of the NPs begins to overlap. Two phenomena are observed in the results: the effect of lamellar formation on nanoplate orientation and the overall phase behavior of the PNCs. The presented research not only expands our knowledge of PNC phase behavior but also introduces a framework to further study the parameters that affect nanoplate alignment in BCP nanocomposites. Our ability to control anisotropic NP orientation in PNCs through self-assembling techniques lends itself to creating multifunctional materials with unique properties for various applications such as photovoltaic cells and barrier coatings.
机译:采用二嵌段共聚物(BCP)来组织和对准各向异性纳米颗粒(NPS)的聚合物纳米复合材料(PNC)具有促进自组装等级结构的可能性。然而,已经完成了有限的研究以了解在BCP中指导非球形NPS组装的参数。在这项工作中,我们建立了一种明确定义的纳米层组系统,以研究二维材料在层状聚(苯乙烯-B-甲基丙烯酸甲基丙烯酸甲酯)(PS-B-PMMA)BCP中的二维材料的对准,其具有与基材平行定向的畴。单分散钆的三氟化钆菱形纳米液掺杂有镱和铒[GDF3:Yb / ER(20/2mol%)]并用磷酸官能化聚乙二醇接枝(PEG-PO(3)H 2)。以化学特异性设计为一个嵌段,纳米板在低体积分数(PHI = 0.0083和PHI = 0.017)的PMMA结构域中对齐。在这些低NP载体上,订购BCP薄片并诱导GDF3:YB / ER纳米板的优先对准。然而,在高体积分数(PHI = 0.050和PHI = 0.064),BCP薄片与各向同性分散的纳米板进行混乱。从有序的BCP系统的转变具有与未对准的纳米间纳米板对齐的纳米间纳入的BCP,与计算的重叠体积分数一致,PHI * = 0.051,其中NP的渗透空间开始重叠。在结果中观察到两种现象:层层形成对纳米板取向和PNC的总相行为的影响。本研究不仅扩大了我们对PNC相行为的知识,还介绍了一种框架,进一步研究了影响BCP纳米复合材料中纳米层对准的参数。我们通过自组装技术控制PNC中的各向异性NP取向的能力,为各种应用等各种应用产生多功能材料,如光伏电池和阻挡涂层。

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